Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

24376–24400 of 26084

HighFDA (Devices)·Z-2595-2021·2021-10-06
Anesthesia Flow Sensors Recalled for Tube Damage and Potential Gas Leaks
GE Healthcare is recalling approximately 310,000 replacement flow sensors for anesthesia machines manufactured before June 2021. The sensors may have damaged tubes that leak, causing incorrect anesthesia delivery to patients.
Product
Flow sensors kept as stand-alone user replaceable spare parts for the GEHC anethesia machines: 2089610-001 FLOW SENSOR, LEGACY VAR ORF BCG (blue, cleanable) 2089610-001-S FLOW SENSOR, LEGACY VAR ORF BCG, SERVICE (blue, cleanable) 2087640-001 FLOW SENSOR, LEGACY VAR ORF AUTOC
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2578-2021·2021-10-06
Aesculap PAS-PORT Surgical Implant Recalled for Deployment Failure
Aesculap Implant Systems is recalling 80 units of the PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM because the implant may fail to deploy during surgery, potentially requiring additional medical intervention.
Product
PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2557-2021·2021-10-06
B. Braun Outlook Pump Set 3 Recalled for Leakage and Medication Delivery Delays
B. Braun Medical is recalling 768 units of Outlook Pump Set 3 infusion sets due to potential leakage that could delay or prevent complete medication delivery and increase risk of bloodstream infection.
Product
OUTLOOK PUMP SET 3 CARESITE LADS 133 IN.-single use, for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: 490564
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2598-2021·2021-10-06
Medical Device: FlexoStretch Patient Lift Leveller May Lose Function During Patient Transfer
Hill-Rom's FlexoStretch Model 3156057 patient lift device may lose the ability to maintain horizontal positioning during patient transfer, risking patient falls. The FDA Class II recall affects 129 units distributed worldwide.
Product
FlexoStretch Model Number: 3156057 - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1026-2021·2021-10-06
Grab & Go Bistro Pimento Cheese Sandwich Recalled for Undeclared Fish Allergen
Modern Distributors, Inc. is recalling Grab & Go Bistro Pimento Cheese Sandwiches because they contain fish that is not declared on the label. The product was distributed through vending machines in Kentucky.
Product
Grab & Go Bistro Pimento Cheese Sandwich 5oz plastic container 1 sandwich per package
Category
Food
Distribution
0 states
HighNHTSA·21V776000·2021-10-05
Spartan RV Chassis K1 and K2 Recalled for Loose Rear Suspension Fasteners
Shyft Group is recalling certain 2020-2022 Spartan K1 and K2 RV chassis because rear suspension fasteners may not have been tightened properly, which could allow the rear axle to shift and increase crash risk. Free repair is available.
Product
SPARTAN — 2021 SPARTAN K2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V770000·2021-10-01
2021 Ford Bronco Passenger Air Bag Vent Deployment Defect
Ford is recalling certain 2021 Bronco vehicles because the passenger air bag vent may open prematurely during deployment, increasing the risk of injury during a crash.
Product
FORD — 2021 FORD BRONCO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V763000·2021-09-30
2021-2022 Starcraft Autumn Ridge Outfitter cooktop fire hazard
Starcraft is recalling 2021-2022 Autumn Ridge Outfitter recreational trailers because the cooktop may invert during furnace operation, increasing fire risk. Dealers will install sealant and plywood panels free of charge.
Product
STARCRAFT — 2022 STARCRAFT AUTUMN RIDGE OUTFITTER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-1008-2021·2021-09-29
Kroger Kale Bags Recalled for Potential Listeria Contamination
The Kroger Co. is recalling Kroger Kale Bags (16 oz) due to potential contamination with Listeria Monocytogenes. The affected product was distributed to retail locations in seven states.
Product
Kroger Kale Bag 16oz plastic bag 8 packages per case
Category
Food
Distribution
7 states
SevereFDA (Food)·F-0988-2021·2021-09-29
Joy Coriander Chutney Recalled for Undeclared Sulfites
Joy Coriander Chutney (8 oz, best by 07/30/22) is being recalled because it contains high levels of undeclared sulfites. Consumers with sulfite sensitivity should not consume this product.
Product
2. "***JOY***Coriander Chutney***NET WT 8 OZ (228g)***07 28 BEST BY 073022***INGREDIENTS: CORIANDER, GREEN CHILLIES, COCONUT, SUGAR, SALT, SPICES, VINEGAR, STABILIZERS (GUAR, TRAGAGANTH AND XANTHAN), CITIRC ACID, SODIUM BENZOATE AS PRESERVATIVE & ARTIFICIAL COLORS (FD&C BLUE 1 &
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-0819-2021·2021-09-29
X Rated Honey For Men Recalled for Undisclosed Tadalafil
Phe Inc is recalling X Rated Honey For Men packets nationwide because the product contains Tadalafil and was marketed without FDA approval. Consumers should stop use immediately.
Product
X RATED HONEY FOR MEN, packaged in 15g packets, 4 packets per box, UPC 6 13682 41232 2
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0827-2021·2021-09-29
Arformoterol Tartrate Inhalation Solution Recall Due to Sterility Assurance
Glenmark Pharmaceuticals is recalling Arformoterol Tartrate Inhalation Solution 15 mcg/2 mL nationwide because the manufacturer lacks assurance of sterility for affected lots.
Product
Arformoterol Tartrate Inhalation Solution 15 mcg*/2 mL For Oral Inhalation Only Rx Only Manufactured by: Glenmark Pharmaceuticals Inc., USA Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430 a) 60x2 mL Sterile Unit-Dose Vials NDC 68462-833-65;
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0830-2021·2021-09-29
Avicel RC-591 NF Bulk Powder Recalled for Microbial Contamination
DuPont Nutrition USA is recalling Avicel RC-591 NF bulk powder (lot #2173766940) due to out-of-specification microbial contamination. The product was distributed as a component in finished drug formulations nationwide.
Product
Avicel RC-591 NF (MCC/Carboxymethylcellulose Sodium) NF, bulk powder, 80.0 KG drum, Manufactured by: DuPont Nutrition USA, Inc., 1301 Ogletown Road, Newark, DE 19711
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1009-2021·2021-09-29
Banquet Cut European Style Cold Smoked Salmon Recalled for Botulinum Risk
Seabear Company is recalling Banquet Cut European Style Cold Smoked Salmon due to potential for growth of Clostridium botulinum. The affected product was distributed in Arizona, California, and Georgia.
Product
Banquet Cut European Style Cold Smoked Salmon, Item Number 2-92845, brand Gerard and Dominique Seafoods, packaged in pouch, net wt. per pouch is random, frozen, UPC of pouch: 2 92845 00250 3. The storage/thawing instructions on the pouch is read in parts: "***KEEP FROZEN UNTIL
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-0820-2021·2021-09-29
Fulvestrant Injection Recall: Lack of Sterility Assurance
Glenmark Pharmaceuticals is recalling Fulvestrant Injection 250 mg/5 mL due to lack of assurance of sterility. The affected product was distributed nationwide in 28,658 cartons across multiple lots.
Product
FULVESTRANT — FULVESTRANT (FULVESTRANT)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1006-2021·2021-09-29
Golden Natural Product Dried Apricots Recalled for Undeclared Sulfites
Golden Natural Product Inc. brand Dried Apricot Subkhon products (with bone and jumbo varieties) are being recalled because they contain high levels of undeclared sulfites. The affected products have lot number GC005 and expiration date 2023.
Product
Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and Golden Natural Product Inc. brand Dried Apricot Subkhon Jumbo, Net Wt. 16 oz (1 lb) 454 g Manufactured and Packed by: Gardencells LLC, Urgut, Samarkand region Republic of Uzbekist
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2480-2021·2021-09-29
Ultrasound Gels and Lotions Recalled Due to Bacterial Contamination
Eco-Med Pharmaceutical, Inc. is recalling ultrasound gels and lotions that may contain bacterial contamination. Products were distributed nationally and internationally.
Product
EcoGel 100 Imaging Gel, EcoGel 200 MultiPurpose Gel (Blue), EcoGel 200 MultiPurpose Gel (CLEAR), and EcoLotion Transmission Lotion 1) 100, 200 gel Intended for use in acoustic coupling of ultrasound transducer to tissue 2) Lotion Ecolotion transmission and massage lotion is in
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2469-2021·2021-09-29
Multiple Ultrasound Gel Products Recalled for Potential Bacterial Contamination
Ultrasound gels sold under multiple brand names have been recalled due to potential bacterial contamination. Approximately 100,114 units distributed nationwide between August 2018 and August 2021 are affected.
Product
Ultrasound Gel labeled under the following brand names: MediChoice Ultrasound Gel, Athena Liquasonic Ultrasound Gel, Eco-Med EcoGel Ultrasound Gel, MAC Medical Supply Ultrasound Gel, Eco-Med EcoGel 200 Blue High Velocity Ultrasound Gel, Eco-Med EcoGel 200 Multi-Purpose Ultrasoun
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2536-2021·2021-09-29
C.R. Bard Foley Catheter Tray recalled for potential packaging defects
C.R. Bard Inc is recalling approximately 29,890 units of Foley catheter trays due to potential packaging defects that may compromise the sterile barrier. No illnesses or injuries have been reported.
Product
Catalog A902916, SureStep" Foley Tray, Lubricath", Urine Meter, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2522-2021·2021-09-29
Foley Catheter Drainage Tray System Packaging Defect Recall
C.R. Bard Inc is recalling a Foley catheter tray system due to potential packaging defects that may compromise the sterile barrier, affecting 1,760 units distributed nationwide.
Product
Catalog A300314A, SureStep" Foley Tray, Bardex" I.C., Complete Care", Drainage Bag, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2519-2021·2021-09-29
ConvaTec DuoDERM wound dressings recalled for potential sterility compromise
ConvaTec is recalling DuoDERM CGF and Extra Thin dressings due to potential open seals that could compromise sterility. Approximately 2.7 million units were distributed internationally.
Product
DuoDERM CGF Dressing 10x10CM (1x5PK) (ICC 187660) DuoDERM Extra Thin Dressing 15X15CM (1X10PK) (ICC 187957) DuoDERM Extra Thin Dressing 10X10CM (1X10PK) (ICC 187955)
Category
Medical Device
Distribution
0 states
HighFDA (Food)·F-1012-2021·2021-09-29
Snickerdoodle Cookies Recalled for Undeclared Soybean Oil
Baker's Corner Bakery is recalling 12-ounce bags of Snickerdoodle Cookies because soybean oil, a sub-ingredient in the shortening, is not declared on the label. Consumers with soy allergies are at risk.
Product
Snickerdoodle Cookie, packed in closed bags, 12oz net wt. The label of affected product is read in parts: "***Snickerdoodle Cookie*** Ingredients: Shepherds Grain Flour (wheat flour, malted barley flour, niacin, reduced iron, thiamine, mononitrate, riboflavin, folic acid), dehyd
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2534-2021·2021-09-29
C.R. Bard Foley Catheter Kits Recalled for Potential Sterile Barrier Defects
C.R. Bard is recalling 960 units of Foley Tray catheter kits (lot NGFR0101) due to potential packaging defects that may compromise the sterile barrier.
Product
Catalog A899916, SureStep" Foley Tray, Lubricath", Drainage Bag, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2516-2021·2021-09-29
Univation X System Tray knee implants recalled for loosening defect
Aesculap is recalling Univation X System Tray knee implants due to a loosening defect that may require revision surgery. All lots nationwide are affected.
Product
Univation X System Tray Sysem knee implant devices as follows: Tray Number/Set Name/Set Number NM1090R Navigation Set ST0560; NM1092R + NM1095R + NM1096R (Tray insert to NM1095R) univation XF ST0540; NM1093R univation XF OPT ST0544
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2539-2021·2021-09-29
SureStep Foley Catheter Tray Recalled for Sterile Barrier Packaging Defect
C.R. Bard Inc is recalling approximately 4830 SureStep Foley catheter trays due to potential packaging defects that could compromise the sterile barrier.
Product
Catalog A902416, SureStep" Foley Tray, Silicone, Urine Meter, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide

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24376–24400 of 26084